A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516366



Internal ID15443659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57352069..57488840hg38UCSC Ensembl
Innerchr15:57644267..57781038hg19UCSC Ensembl
Innerchr15:55431559..55568330hg18UCSC Ensembl
Innerchr15:55431559..55568330hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38136772
hg19136772
hg18136772
hg17136772
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688615, nssv683558, nssv682044, nssv668668, nssv660246, nssv705716, nssv692279, nssv655031, nssv667792, nssv692257, nssv687907
Samples
Known GenesCGNL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516366
Frequency
Sample Size2026
Observed Gain10
Observed Loss1
Observed Complex0
Frequencyn/a


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